Canonical Allele Identifier: CA2383551759
Gene: APP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.25892065_25892066delinsAG , CM000683.2:g.25892065_25892066delinsAG GRCh38
NC_000021.8:g.27264377_27264378delinsAG , CM000683.1:g.27264377_27264378delinsAG GRCh37
NC_000021.7:g.26186248_26186249delinsAG NCBI36
NG_007376.1:g.283755_283756delinsCT
NG_007376.2:g.284063_284064delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000707132.1:n.2032-198_2032-197delinsCT
ENST00000707133.1:n.462-198_462-197delinsCT
ENST00000707134.1:n.731-198_731-197delinsCT
ENST00000346798.8:c.2065-198_2065-197delinsCT MANE Select ENSP00000284981.4:n.2065-198_2065-197delinsCT
ENST00000346798.7:c.2065-198_2065-197delinsCT ENSP00000284981.4:n.2065-198_2065-197delinsCT
ENST00000348990.9:c.1840-198_1840-197delinsCT ENSP00000345463.5:n.1840-198_1840-197delinsCT
ENST00000354192.7:c.1672-198_1672-197delinsCT ENSP00000346129.3:n.1672-198_1672-197delinsCT
ENST00000357903.7:c.2008-198_2008-197delinsCT ENSP00000350578.3:n.2008-198_2008-197delinsCT
ENST00000358918.7:c.2011-198_2011-197delinsCT ENSP00000351796.3:n.2011-198_2011-197delinsCT
ENST00000359726.7:c.1735-198_1735-197delinsCT ENSP00000352760.4:n.1735-198_1735-197delinsCT
ENST00000439274.6:c.1897-198_1897-197delinsCT ENSP00000398879.2:n.1897-198_1897-197delinsCT
ENST00000440126.7:c.1993-198_1993-197delinsCT ENSP00000387483.2:n.1993-198_1993-197delinsCT
ENST00000464867.1:n.412-198_412-197delinsCT
NM_000484.3:c.2065-198_2065-197delinsCT NP_000475.1:n.2065-198_2065-197delinsCT
NM_001136016.3:c.1993-198_1993-197delinsCT NP_001129488.1:n.1993-198_1993-197delinsCT
NM_001136129.2:c.1672-198_1672-197delinsCT NP_001129601.1:n.1672-198_1672-197delinsCT
NM_001136130.2:c.1897-198_1897-197delinsCT NP_001129602.1:n.1897-198_1897-197delinsCT
NM_001136131.2:c.1735-198_1735-197delinsCT NP_001129603.1:n.1735-198_1735-197delinsCT
NM_001204301.1:c.2011-198_2011-197delinsCT NP_001191230.1:n.2011-198_2011-197delinsCT
NM_001204302.1:c.1954-198_1954-197delinsCT NP_001191231.1:n.1954-198_1954-197delinsCT
NM_001204303.1:c.1786-198_1786-197delinsCT NP_001191232.1:n.1786-198_1786-197delinsCT
NM_201413.2:c.2008-198_2008-197delinsCT NP_958816.1:n.2008-198_2008-197delinsCT
NM_201414.2:c.1840-198_1840-197delinsCT NP_958817.1:n.1840-198_1840-197delinsCT
NM_000484.4:c.2065-198_2065-197delinsCT MANE Select NP_000475.1:n.2065-198_2065-197delinsCT
NM_001136129.3:c.1672-198_1672-197delinsCT NP_001129601.1:n.1672-198_1672-197delinsCT
NM_001136130.3:c.1897-198_1897-197delinsCT NP_001129602.1:n.1897-198_1897-197delinsCT
NM_001204301.2:c.2011-198_2011-197delinsCT NP_001191230.1:n.2011-198_2011-197delinsCT
NM_001204302.2:c.1954-198_1954-197delinsCT NP_001191231.1:n.1954-198_1954-197delinsCT
NM_001204303.2:c.1786-198_1786-197delinsCT NP_001191232.1:n.1786-198_1786-197delinsCT
NM_201413.3:c.2008-198_2008-197delinsCT NP_958816.1:n.2008-198_2008-197delinsCT
NM_201414.3:c.1840-198_1840-197delinsCT NP_958817.1:n.1840-198_1840-197delinsCT
NM_001136131.3:c.1735-198_1735-197delinsCT NP_001129603.1:n.1735-198_1735-197delinsCT
NM_001385253.1:c.1897-198_1897-197delinsCT NP_001372182.1:n.1897-198_1897-197delinsCT